[Management of hemostasis abnormalities in patients with liver failure]

Transfus Clin Biol. 2013 May;20(2):249-54. doi: 10.1016/j.tracli.2013.02.007. Epub 2013 Mar 21.
[Article in French]

Abstract

Patients with end-stage liver disease have complex alterations that involve all components of hemostasis, with changes both in prohemostatic and in antihemostatic pathways. Routine haemostasis tests such as prothrombin time and platelet count are unable to reflect a bleeding tendency. Bleeding complications are much less related to abnormal hemostasis than previously thought, with portal hypertension playing a more critical role. Systematic prophylactic measures based upon the use of fresh frozen plasma and/or platelet concentrates to improve or correct the abnormalities of the routine coagulation tests are most often inappropriate and may occasionally be deleterious.

Publication types

  • Review

MeSH terms

  • Blood Coagulation Disorders / diagnosis
  • Blood Coagulation Disorders / drug therapy
  • Blood Coagulation Disorders / etiology
  • Blood Coagulation Disorders / therapy*
  • Blood Coagulation Factors / therapeutic use
  • Blood Coagulation Tests
  • Blood Transfusion
  • Combined Modality Therapy
  • Hemorrhagic Disorders / drug therapy
  • Hemorrhagic Disorders / etiology
  • Hemorrhagic Disorders / therapy
  • Humans
  • Hypertension, Portal / blood
  • Hypertension, Portal / etiology
  • Liver Failure / blood
  • Liver Failure / complications*
  • Liver Failure / physiopathology
  • Metabolic Syndrome / blood
  • Metabolic Syndrome / complications
  • Plasma
  • Platelet Transfusion
  • Thrombocytopenia / etiology
  • Thrombocytopenia / therapy
  • Thrombophilia / etiology
  • Thrombophilia / therapy

Substances

  • Blood Coagulation Factors